US2158959A - Hydroxy-alkyl ethers of tertiary - Google Patents
Hydroxy-alkyl ethers of tertiary Download PDFInfo
- Publication number
- US2158959A US2158959A US2158959DA US2158959A US 2158959 A US2158959 A US 2158959A US 2158959D A US2158959D A US 2158959DA US 2158959 A US2158959 A US 2158959A
- Authority
- US
- United States
- Prior art keywords
- tertiary
- hydroxy
- phenol
- beta
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 125000002768 hydroxyalkyl group Chemical group 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 description 30
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 28
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 22
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 16
- SZXQTJUDPRGNJN-UHFFFAOYSA-N Dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 12
- 125000004432 carbon atoms Chemical group C* 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000003513 alkali Substances 0.000 description 8
- NRZWYNLTFLDQQX-UHFFFAOYSA-N p-tert-Amylphenol Chemical compound CCC(C)(C)C1=CC=C(O)C=C1 NRZWYNLTFLDQQX-UHFFFAOYSA-N 0.000 description 8
- 241000257226 Muscidae Species 0.000 description 6
- 125000002947 alkylene group Chemical group 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 150000002989 phenols Chemical class 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-Chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 4
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 4
- CYEKUDPFXBLGHH-UHFFFAOYSA-N 3-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC(O)=C1 CYEKUDPFXBLGHH-UHFFFAOYSA-N 0.000 description 4
- LYKRIFJRHXXXDZ-UHFFFAOYSA-N 4-(4-hydroxybutoxy)butan-1-ol Chemical compound OCCCCOCCCCO LYKRIFJRHXXXDZ-UHFFFAOYSA-N 0.000 description 4
- XENVCRGQTABGKY-ZHACJKMWSA-N Chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 4
- 238000007710 freezing Methods 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 150000003944 halohydrins Chemical class 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 230000001965 increased Effects 0.000 description 4
- 239000003350 kerosene Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- VZIQXGLTRZLBEX-UHFFFAOYSA-N 2-Chloro-1-propanol Chemical compound CC(Cl)CO VZIQXGLTRZLBEX-UHFFFAOYSA-N 0.000 description 2
- LDLCZOVUSADOIV-UHFFFAOYSA-N 2-bromoethanol Chemical compound OCCBr LDLCZOVUSADOIV-UHFFFAOYSA-N 0.000 description 2
- 229910014033 C-OH Inorganic materials 0.000 description 2
- 229910014570 C—OH Inorganic materials 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000006266 etherification reaction Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000004508 fractional distillation Methods 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- -1 phenol compound Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000002588 toxic Effects 0.000 description 2
- 231100000167 toxic agent Toxicity 0.000 description 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented May 16 1939 HYDROXY-ALKYL ETHERS OF TERTIARY- ALKYL PHENOLS Gerald H. Coleman and John W. Zemba, Midland, Mich., assignors to The Dow Chemical Company, Midland, Mich., a corporation of Michigan No Drawing. Application January 12, 1938, 7 Serial N0. 184,561
13 Claims. (01. 260-413) a This invention concerns hydroxyl-allwl ethers of tertiary-alkyl phenol compounds having the formula m wherein R represents an alkylene group containing from 2 to 4 carbon atoms, inclusive, and n is an integer not greater than 2.
We have prepared members of this class or compounds, determined certain physical charac- 1 teristics thereof whereby they may be readily identified, and found that they are particularly useful in the preparation of compositions for the control of household insect pests, such as fly sprays. v
These new compounds may be prepared by reacting a suitable phenol compound with an halohydrin, e. g. ethylene-bromohydrin, propylenechlorohydrin, etc., in the presence of a suitable alkali, e. g. NaOH, KOH, etc.
.In preparing our new compounds, the phenol may be'dissolved in aqueous alkali and the halohydri'an added thereto at a reaction temperature with stirring. If desired, however, the reaction may be carried out by first mixing the phenol with the halohydrin and subsequently adding thereto the alkali. While any suitable quantities of reactants may be employed, good yields of the desired products can be obtained when equimolecular proportions of" reactants are used.
35 The reaction may be conveniently carried out at the refluxing temperature of the mixture, but lower, or higher temperatures may be employed. In certain cases where the reactants are not readily solublein aqueous alkali, alcohol or other 0 water-miscible organic solvent may be added to the-reaction mixture; 'Following' completion of the reaction the mixture is allowed to stand and separate'into layers, the oily layer being subsequently separated, and the desired compound isolated therefrom by fractional distillation under reduced pressure orotherwise.
' Other methods by which the compounds may be prepared are; (1) the condensation of the alkyl- 56 ene ox ides with suitable tertiary-alkyl phenols,
and (2) the etherification of the dihydroxy paraflin hydracarbons with the tertiary-alkyl substituted phenols.
The following examples describe the prepara- 66 tion of certain representative members of our new group of compounds, but are not to be construed as limiting the invention:
Example 1 150 grams (1 mol) of 4-tertiary-buty1 phenol 5 and 192 grams (1 mol) of a 42 per cent aqueous azeotrope of ethylene chlorohydrin were mixed together and 133 grams of a 30 per cent aqueous sodium hydroxide solution added thereto over a period of one hour at temperatures gradually increasing from 25 to 42 C. Stirring was maintained for an additional hour after which the reaction batchwas allowed to stand for 16 hours at room temperature. An oily layer separated therefrom and was fractionally distilled, whereby 145 grams (0.748 mol) of the beta-hydroxy-ethyl ether of 4-tertiary-butyl phenol was obtained as a water-white oil boiling at 126.5127.5 C. at 4 millimeters pressure, freezing at approximately 15 C. and having a specific gravity of 1.015 at 20/4 C. This compound was substantially insoluble in water but somewhat soluble in most organic solvents.
Example 2 Example 3 2 mols of 4-tertiary-butyl phenol, 2 mols of sodium hydroxide, and 400 milliliters of water were mixed together, and 2 mols of propylene 4o chlorohydrin in the form of a 51 per cent aqueous azeotrope gradually added thereto overa period of 2 hours and at temperatures gradually increas-- ing from 79 to 96.5 C. The reaction mixture was refluxed for a short time after the addition 45 of the chlorohydrin, cooled, acidified, and the resulting oil separated therefrom. The latter was washed with water and distilled whereby there was obtained 1.4 mols of the hydroxy-propyl ether of 4-tertiary-butyl phenol as a white crystalline solid, melting at 45 C., and boiling at 150-155 C. at 10 millimeters pressure.
Ewample 4 In a similar manner Z-tertiary-butyl phenol was reacted with sodium hydroxide and ethylene chlorohydrin whereby there was obtained the beta-hydroxy-ethyl ether of 2-tertiary-butyl phenol, a water-white liquid boiling at 110-113 C. at 4 millimeters pressure, freezing at approximately 1'7.5 C., and having a specific gravity of 1.021 at 20/4 C.
Among other hydroxy-alkyl ethers which may be prepared by substituting other tertiary-akyl substituted phenol compounds for those shown in the examples are beta-hydroxy-ethyl ether of 3-tertiary-butyl phenol, beta-hydroxy-ethyl ether of Z-tertiary-amyl phenol, beta-hydroxy-ethyl ether of 3tertiary-amyl phenol, hydroxy-propyl ether of Z-tertiary-amyl phenol, hydroxy-propyl ether of 3-tertiary-butyl phenol, hydroxy-propyl ether of 4-tertiary-amyl phenol, hydroxy-butyl ether of 4-tertiary-butyl phenol, hydroxy-butyl ether of 4-tertiary-amyl phenol, etc.
Certain of the compounds described in the fore going examples have been tested by the Peet- Grady method (Soap, 8, No. 4, 1932) and found to be particularly valuable as fly spray toxics. For example, a 3 per cent solution of betahydroxy-ethyl ether of 4-tertiary-butyl phenol in kerosene, when tested against house flies, was found to give in excess of a per cent knockdown and an average kill of over 45 per cent in 24 hours. A 3 per cent solution of beta-hydroxyethyl ether of 4-tertiary-amyl phenol in kerosene killed approximately 45 per cent of house flies contacted therewith when tested in a similar manner. Likewise, the hydroxy-propyl ether of 4-tertiary-butyl phenol was found to kill'approximately 30 per cent of house flies contacted therewith.
This application is a continuationin-part of our co-pending application Serial Number 127,- 177, filed February 23, 1937.
Other modes of applying the principle of our invention may be employed instead of those explained, change being made as regards the materials employed provided the products described in the following claims be thereby obtained.
We therefore particularly point out and distinctly claim as our invention:
1. A compound having the formula wherein R represents an alkylene group containing from 2 to 4 carbon atoms, inclusive, and n is an integer not greater than 2.
2. A compound having the formula wherein n is an integer not greater than 2.
3. A compound having the formula wherein n is an integer not greater than 2, one R represents hydrogen, and the other R represents a member of the group consisting of methyl and hydrogen.
4. A compound having the formula o-R-OH I CHa-C-CHa CnH2n+1 wherein R represents an alkylene group containing from 2 to 4 carbon atoms, inclusive, and n is an integer not greater than 2.
5. A compound having the formula CHa-C-CHa wherein R represents an alkylene radical containing from 2 to 4 carbon atoms, inclusive. 7. A compound having the formula wherein R represents an alkaylene group containing from 2 to 4 carbon atoms, inclusive.
8. A compound having the formula C Ha-C-OH;
CzHa
wherein R represents an alkylene radical containing from 2 to 4 carbon atoms, inclusive.
9. A beta-hydroxy-ethyl ether of tertiary-butyl phenol.
10. A beta-hydroxy-ethyl ether of tertiaryamyl phenol.
11. The beta-hydroxy-ethyl ether of 4-tertiarybutyl phenol.
12. The beta-hydroxy-ethyl ether of 4-tertiary-amyl phenol.
13. The hydroxy-propyl ether of 4-tertiarybutyl phenol.
GERALD H. COLEMAN. JOHN W. ZEMBA.
Publications (1)
Publication Number | Publication Date |
---|---|
US2158959A true US2158959A (en) | 1939-05-16 |
Family
ID=3430207
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US2158959D Expired - Lifetime US2158959A (en) | Hydroxy-alkyl ethers of tertiary |
Country Status (1)
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US (1) | US2158959A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2451149A (en) * | 1942-11-16 | 1948-10-12 | Nipa Lab Ltd | Manufacture of materials resistant to or active against microorganisms |
US2453351A (en) * | 1945-07-26 | 1948-11-09 | Wyandotte Chemicals Corp | Composition for inhibiting foam |
US2453352A (en) * | 1945-07-26 | 1948-11-09 | Wyandotte Chemicals Corp | Composition for inhibiting foam |
US2486744A (en) * | 1947-01-31 | 1949-11-01 | Eversharp Inc | Composition of matter |
US4816491A (en) * | 1980-01-22 | 1989-03-28 | Frank M. Berger | Treatment of allergic conditions using indanyloxy-alkanol derivatives |
US5021460A (en) * | 1980-01-22 | 1991-06-04 | Frank M. Berger | P-alkyl phenoxy alkanols for the treatment of allergic conditions |
-
0
- US US2158959D patent/US2158959A/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2451149A (en) * | 1942-11-16 | 1948-10-12 | Nipa Lab Ltd | Manufacture of materials resistant to or active against microorganisms |
US2453351A (en) * | 1945-07-26 | 1948-11-09 | Wyandotte Chemicals Corp | Composition for inhibiting foam |
US2453352A (en) * | 1945-07-26 | 1948-11-09 | Wyandotte Chemicals Corp | Composition for inhibiting foam |
US2486744A (en) * | 1947-01-31 | 1949-11-01 | Eversharp Inc | Composition of matter |
US4816491A (en) * | 1980-01-22 | 1989-03-28 | Frank M. Berger | Treatment of allergic conditions using indanyloxy-alkanol derivatives |
US5021460A (en) * | 1980-01-22 | 1991-06-04 | Frank M. Berger | P-alkyl phenoxy alkanols for the treatment of allergic conditions |
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